ZFP30 ZFP30 zinc finger protein
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
48 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ZNF745 |
MIM | 617317 OMIM |
HGNC | HGNC:29555 HGNC |
Ensembl | ENSG00000120784 Ensembl |
AllianceGenome | HGNC:29555 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000351218.6 | hg38 | chr19 | 37,631,009 | 37,655,412 | 24,404 |
ENST00000589018.5 | hg38 | chr19 | 37,613,749 | 37,654,729 | 40,981 |
ENST00000514101.6 | hg38 | chr19 | 37,632,488 | 37,656,261 | 23,774 |
ENST00000684514.1 | hg38 | chr19 | 37,631,006 | 37,655,465 | 24,460 |
ENST00000589018.5 | hg19 | chr19 | 38,104,650 | 38,145,630 | 40,981 |
ENST00000684514.1 | hg19 | chr19 | 38,121,907 | 38,146,366 | 24,460 |
ENST00000351218.6 | hg19 | chr19 | 38,121,910 | 38,146,313 | 24,404 |
ENST00000514101.6 | hg19 | chr19 | 38,123,389 | 38,147,162 | 23,774 |
Genome browser